Getting your devices ready for MDR compliance – a clinical approach and orthopaedic device manufacturers’ perspective
On 26 May 2017, the Medical Devices Regulation (MDR 2017/745) was published, with the aim of replacing the current Medical Devices Directive (MDD 93/43/EC). Following a transition period of 3 years, this regulation will be applied in full from 26 May 2020. This article describes and discusses the...
Main Authors: | Peter Fennema, Hassan Achakri |
---|---|
Format: | Article |
Language: | English |
Published: |
AboutScience Srl
2019-07-01
|
Series: | AboutOpen |
Subjects: | |
Online Access: | https://journals.aboutscience.eu/index.php/aboutopen/article/view/294 |
Similar Items
-
Orthopaedic device manufacturers’ perspective on MDR compliance
by: Peter Fennema, et al.
Published: (2021-05-01) -
Enhancing Healthcare Decision-Making Process: Findings from Orthopaedic Field
by: Irene Schettini, et al.
Published: (2020-11-01) -
Providing clinical evidence under the MDR 2017/745: New challenges for manufacturers in medical device industry
by: Ivanovska Elena, et al.
Published: (2019-01-01) -
Bacteriophage therapy as a treatment strategy for orthopaedic-device-related infections: where do we stand?
by: J Onsea, et al.
Published: (2020-05-01) -
The integration of a Podiatrist into an orthopaedic department: a cost-consequences analysis
by: Tom P. Walsh, et al.
Published: (2017-10-01)